WHO Drug Information Vol. 15, No. 2, 2001
(2001; 91 pages) View the PDF document
Table of Contents
Open this folder and view contentsPersonal Perspectives
Open this folder and view contentsReports on Individual Drugs
Open this folder and view contentsVaccines and Biomedicines
Close this folderCurrent Topics
View the documentImplementation of the ICH common technical document
View the documentMonitoring the emergence of antiretroviral resistance
View the documentPharmaceutical legislation review
View the documentArgentina takes action against black market pharmaceuticals
View the documentPharmacopoeial quality of drugs supplied by Nigerian pharmacies
View the documentUse of placebo in clinical trials
View the documentWHO guidelines on good clinical practice reviewed
Open this folder and view contentsGeneral Information
Open this folder and view contentsRegulatory and Safety Matters
Open this folder and view contentsATC/DDD Classification
Open this folder and view contentsEssential Drugs
Open this folder and view contentsRecent Publications and Sources of Information
View the documentInternational Nonproprietary Names for Pharmaceutical Substances (INN)
View the documentDénominations communes internationales des Substances pharmaceutiques (DCI)
View the documentDenominaciones Comunes Internacionales para las Sustancias Farmacéuticas (DCI)
View the documentAmendments to previous lists/Modifications apportées aux listes antérieures/Modificaciones a las listas anteriores
View the documentAnnexes
 

Pharmaceutical legislation review

The European Commission has now published a proposal to review pharmaceutical legislation. One objective of the review is to reinforce and improve access to patient oriented and controlled information, including the development of Good Information Practice. In addition, a pilot system will be set up to ensure the availability of patient oriented and valid information on authorized prescription drugs for three types of illnesses - AIDS, diabetes, asthma and chronic bronchitis. These long term, chronic diseases have been chosen based on strong patient demand for information and will cover types of drugs used where these are the same throughout Europe.

Companies will be required to notify the information they intend to distribute to the European Medicines Evaluation Agency for appraisal and will be subject to a code of conduct to be worked out by the Commission in cooperation with industry, patients and Member Countries.

Reference: Pharmaceutical Legislation Review 2001 at http://pharmacos.eudra.org/F2/home.html

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Last updated: May 3, 2013